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Erscheinungsjahr
Autor/in
- Oyen, Florian
- Schneppenheim, Reinhard 11
- Obser, Tobias 6
- Budde, U 4
- Ulrich, Budde 4
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Sprache
14 Einträge gefunden
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Difficulties in diagnosing congenital thrombotic thrombocytopenic purpura.
2010 - Forschungsinformationssystem des UKE -
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The problem of novel FVIII missense mutations for haemophilia A genetic counseling.
2009 - Forschungsinformationssystem des UKE -
Response to DDAVP in children with von Willebrand disease type 2.
- Schneppenheim, Reinhard
- Budde, U
- Beutel, Karin
- Hassenpflug, W-A
- Hauch, H
- Obser, Tobias
- Oyen, Florian
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Genetic defects in von Willebrand disease type 3 in Indian and Greek patients.
2008 - Forschungsinformationssystem des UKE -
An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary.
2008 - Forschungsinformationssystem des UKE -
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A common origin of the 4143insA ADAMTS13 mutation.
- Schneppenheim, Reinhard
- Hovinga, Kremer
- Johanna, A
- Becker, Tim
- Ulrich, Budde
- Karpman, Diana
- Brockhaus, Wolfgang
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Intracranial hemorrhage in a term newborn with severe von Willebrand disease type 3 associated with sinus venous thrombosis.
- Wetzstein, Viola
- Ulrich, Budde
- Oyen, Florian
- Ding, Xiaoqi
- Herrmann, Jochen
- Liebig, Birte
- Schneppenheim, Reinhard
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Gene conversions are a common cause of von Willebrand disease.
2005 - Forschungsinformationssystem des UKE -
von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP.
- Schneppenheim, Reinhard
- Ulrich, Budde
- Oyen, Florian
- Angerhaus, Dorothea
- Aumann, Volker
- Drewke, Elke
- Hassenpflug, Wolf